MICROspecialties recalls Synerget: I Pack Injection Kit Tray (Model 18060) due to potential infection from improper sterilization. Affected units sold with specific lot numbers.
Could not confirm products were exposed to the proper sterilization cycle can potentially cause post operative wound infection or injection site infection.
MICROspecialties is recalling their Synergetics I Pack Injection Kit Tray (Model 18060) because it may not have been properly sterilized, which could lead to post-surgery infections. This affects medical professionals using the kit for eye injections.
The kit may not have gone through the correct sterilization process, which could lead to infections at the injection site or after surgery. This happens because the sterilization cycle wasn't confirmed to be effective.
Medical professionals who use this injection kit for ophthalmic procedures are most at risk. The recall applies to specific lot numbers sold with the model 18060.
Check for the model number 18060 on the tray. Affected units have lot number P62764979R and were sold with the unique device identifier 10841305101064.
Look for model number 18060 and lot number P62764979R on the tray.
The kit may not have been properly sterilized, which could lead to post-surgery infections.
Check the model number and lot number to see if it's affected; no specific action is required if it's not in the recall list.
The recall is for potential infection risk, not immediate injury. The hazard does not involve death or serious injury in normal use.
We’ve drafted a message you can send MICROspecialties to request your refund or repair — edit it as you like.
Subject: Recall Z-2333-2024 — MICROspecialties MICROspecialties Hello, I own a MICROspecialties that is covered by recall Z-2333-2024 from MICROspecialties. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
